Publications
Found 4 results
Filters: Author is X.D. Kong [Clear All Filters]
“Mutation analyses and prenatal diagnosis in families of X-linked severe combined immunodeficiency caused by IL2Rγ gene novel mutation”, vol. 14, pp. 6164-6172, 2015.
, “A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract”, vol. 14, pp. 426-432, 2015.
, “Prenatal diagnosis of Chinese families with phenylketonuria”, vol. 14, pp. 14615-14628, 2015.
, “Mutation analysis and prenatal diagnosis for three families affected by isolated methylmalonic aciduria”, vol. 13, pp. 8234-8240, 2014.
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